BUY DIPHENIDINE ONLINE
Buy Diphenidine Online
A chemical compound known as diphenidine has the IUPAC or systematic name of (1-(1,2-diphenylethyl)piperidine. Its activity is comparable to that of an NMDA receptor channel blocker. Diphenidine has the chemical formula C19H23N, and its average mass is calculated to be 265.392609 Da, while its monoisotopic mass is calculated to be 265.183044 Da.
Diphenidine has a number of chemical and physical properties, such as a heavy atom count of 23, a topological polar surface area of 23.5, a count of 1 for covalently bonded units, a count of 1 for 3D feature acceptors, a count of 1 for 3D feature donors, a count for 3D feature cations, a count for 3D feature rings, and an effective rotor count of 4.2.
An in-vitro NMDA receptor antagonist is known as Diphenidine, also known as DND or 1,2-Diphenylethylpiperidine. These abbreviations refer to 1-(1,2-Diphenylethyl)piperidine. Ketamine, methoxetamine, and 4-meO-PCP are only a few examples of further well-known NMDA receptor antagonists.
The action of this molecule is akin to that of these other NMDA antagonists because of the nature of its chemical structure; nonetheless, the chemical structure of this molecule is entirely novel.
Researchers interested in investigating the molecule will need to have access to a high-quality set of scales that are capable of correctly weighing quantities of material as low as 50-100 mg, just as any competent laboratory should have.
Although Diphenidine is a relatively close counterpart of chemicals such as Lefetamine and MT-45, it is not known to have any affinity for the opioid receptors, in contrast to the aforementioned medicines.
Diphenidine, like all of the other chemicals that we sell, is not permitted to be used in any kind of in-vivo research (that is, not in humans or animals), nor is it permitted to be used in clinical trials; as a result, immediate medical attention should be sought if the chemical is accidentally consumed. Please make sure that you use appropriate skin, eye, and clothing protection, as well as follow the normal safety standards that are required in the laboratory.
A dissociative anesthetic known as diphenidine has been marketed to consumers as a “designer drug.” The synthesis of diphenidine was initially described in 1924, and it used a Bruylants reaction that was comparable to the one that would later be utilized to find phencyclidine in 1956. This discovery was made possible by the use of an analogous reaction.
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